Canonical Allele Identifier: CA2794437752

Gene: C1R

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7086428A>C , CM000674.2:g.7086428A>C	GRCh38
NG_062465.1:g.11180T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647956.2:c.1068T>G MANE Select	ENSP00000497341.1:p.Ala356=
ENST00000648162.1:n.1040T>G
ENST00000649804.1:c.162T>G	ENSP00000497938.1:p.Ala54=
ENST00000535233.6:c.966T>G	ENSP00000438636.3:p.Ala322=
ENST00000536053.6:c.1110T>G	ENSP00000444271.3:p.Ala370=
ENST00000540394.5:n.2133T>G
ENST00000542285.5:c.1068T>G	ENSP00000438615.2:p.Ala356=
ENST00000602298.2:n.1417T>G
NM_001733.4:c.1068T>G	NP_001724.3:p.Ala356=
NM_001354346.1:c.1110T>G	NP_001341275.1:p.Ala370=
NM_001733.6:c.1068T>G	NP_001724.4:p.Ala356=
NM_001733.7:c.1068T>G MANE Select	NP_001724.4:p.Ala356=
NM_001354346.2:c.1110T>G	NP_001341275.1:p.Ala370=